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The Journal of Biological Chemistry
|
June 30, 2001
Molecular and Biochemical Characterization of Rat epsilon -N-Trimethyllysine Hydroxylase, the First Enzyme of Carnitine Biosynthesis
F M Vaz, R Ofman, K Westinga, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder
R J Wanders, H Schumacher, J Heikoop, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Major hyperpipecolataemia in a normal adult
C Vallat, S Denis, H Bellet, et al.
Journal of Lipid Research
|
February 13, 2001
Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency
S Ferdinandusse, H Overmars, S Denis, et al.
Biological Chemistry
|
November 5, 1997
Subcellular localization of dihydropyrimidine dehydrogenase
A B Van Kuilenburg, H Van Lenthe, R J Wanders, et al.
European Journal of Biochemistry
|
August 1, 1997
Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiae
N Verleur, Y Elgersma, C W Van Roermund, et al.
The Journal of Biological Chemistry
|
August 24, 1999
MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency
K A Sacksteder, J C Morrell, R J Wanders, et al.
The Journal of Clinical Investigation
|
August 6, 1998
Molecular basis of hepatic carnitine palmitoyltransferase I deficiency
L IJlst, H Mandel, W Oostheim, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency
H J ten Brink, R J Wanders, F Stellaard, et al.
American Journal of Human Genetics
|
April 1, 1993
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
N Shimozawa, Y Suzuki, T Orii, et al.
Page
of 50
Search research articles
Search
Showing results (131-140 of 497) with videos related to
Sort By:
Page
of 50
The Journal of Biological Chemistry
|
June 30, 2001
Molecular and Biochemical Characterization of Rat epsilon -N-Trimethyllysine Hydroxylase, the First Enzyme of Carnitine Biosynthesis
F M Vaz, R Ofman, K Westinga, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder
R J Wanders, H Schumacher, J Heikoop, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Major hyperpipecolataemia in a normal adult
C Vallat, S Denis, H Bellet, et al.
Journal of Lipid Research
|
February 13, 2001
Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency
S Ferdinandusse, H Overmars, S Denis, et al.
Biological Chemistry
|
November 5, 1997
Subcellular localization of dihydropyrimidine dehydrogenase
A B Van Kuilenburg, H Van Lenthe, R J Wanders, et al.
European Journal of Biochemistry
|
August 1, 1997
Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiae
N Verleur, Y Elgersma, C W Van Roermund, et al.
The Journal of Biological Chemistry
|
August 24, 1999
MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency
K A Sacksteder, J C Morrell, R J Wanders, et al.
The Journal of Clinical Investigation
|
August 6, 1998
Molecular basis of hepatic carnitine palmitoyltransferase I deficiency
L IJlst, H Mandel, W Oostheim, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency
H J ten Brink, R J Wanders, F Stellaard, et al.
American Journal of Human Genetics
|
April 1, 1993
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
N Shimozawa, Y Suzuki, T Orii, et al.
Page
of 50